CH177469A - Process for the preparation of a new monoazo dye. - Google Patents
Process for the preparation of a new monoazo dye.Info
- Publication number
- CH177469A CH177469A CH177469DA CH177469A CH 177469 A CH177469 A CH 177469A CH 177469D A CH177469D A CH 177469DA CH 177469 A CH177469 A CH 177469A
- Authority
- CH
- Switzerland
- Prior art keywords
- preparation
- monoazo dye
- new monoazo
- dye
- new
- Prior art date
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09B—ORGANIC DYES OR CLOSELY-RELATED COMPOUNDS FOR PRODUCING DYES, e.g. PIGMENTS; MORDANTS; LAKES
- C09B29/00—Monoazo dyes prepared by diazotising and coupling
- C09B29/24—Monoazo dyes prepared by diazotising and coupling from coupling components containing both hydroxyl and amino directing groups
- C09B29/28—Amino naphthols
- C09B29/30—Amino naphtholsulfonic acid
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Coloring (AREA)
Description
Verfahren zur Herstellung eines neuen Monoazofarbstoffes. Vorliegendes Patent bezieht sich auf ein Verfahren zur Herstellung eines neuen Mono azofarbstoffes, dadurch gekennzeichnet, dass man die Diazoverbindung von Anthranilsäure mit der 2-Methogyacetylamino-5-naphthol-7- sulfosäure kuppelt.
Der erhaltene Farbstoff stellt ein rot braunes wasserlösliches Pulver dar und färbt die animalische Faser in sehr egalen, leb haften Orangetönen von sehr guter Licht echtheit.
Beispiel: 13,7 kg Anthranilsäure werden in der üblichen Weise diazotiert und die erhaltene Diazolösungwird mit einer mit überschüssigem Natriumbicarbonat versetzten Lösung von 32 kg der 2-Methogyacetylamino-5-naphthol- 7-sulfosäure gekuppelt. Der gebildete Farb stoff wird in üblicher Weise isoliert und ge trocknet.
Process for the preparation of a new monoazo dye. The present patent relates to a process for the preparation of a new mono azo dye, characterized in that the diazo compound of anthranilic acid is coupled with 2-methogyacetylamino-5-naphthol-7-sulfonic acid.
The dye obtained is a red-brown water-soluble powder and dyes the animal fiber in very level, vivid orange tones of very good light fastness.
Example: 13.7 kg of anthranilic acid are diazotized in the usual way and the diazo solution obtained is coupled with a solution of 32 kg of 2-methogyacetylamino-5-naphthol-7-sulfonic acid to which excess sodium bicarbonate has been added. The color formed is isolated in the usual way and dried ge.
Claims (1)
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DE177469X | 1933-01-24 | ||
CH172366T | 1934-01-09 |
Publications (1)
Publication Number | Publication Date |
---|---|
CH177469A true CH177469A (en) | 1935-05-31 |
Family
ID=25719193
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CH177469D CH177469A (en) | 1933-01-24 | 1934-01-09 | Process for the preparation of a new monoazo dye. |
Country Status (1)
Country | Link |
---|---|
CH (1) | CH177469A (en) |
-
1934
- 1934-01-09 CH CH177469D patent/CH177469A/en unknown
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